Senior Validation Specialist
2 weeks ago
Job Title : Senior Computer Systems Validation (CSV Skillset)
Location : Raritan, NJ (Onsite)
Duration: 6 months Contract
Job Description:
Experience in computer systems validation, GXP regulatory knowledge and good documentation methods and CSA approaches and risk-based validation required.
Prior experience in SAP ECC/S4 HANA system validation, Solman/ChaRM change control process, JIRA/XRAY/qTEST tools for validation required.
Test automation tools and methods, authoring and/or reviewing validation deliverables such as Compliance Plan, Summary Report, Test Protocols, Test Scripts, Requirements and Trace Matrix is required.
Experience working in Agile methodology and tools is required.
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Senior Validation Specialist
2 weeks ago
Raritan, United States K-Tek Resourcing LLC Full timeJob Title : Senior Computer Systems Validation (CSV Skillset) Location : Raritan, NJ (Onsite) Duration: 6 months Contract Job Description: Experience in computer systems validation, GXP regulatory knowledge and good documentation methods and CSA approaches and risk-based validation required. Prior experience in SAP ECC/S4 HANA system validation,...
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Senior Validation Specialist
7 days ago
Raritan, United States K-Tek Resourcing LLC Full timeJob Title : Senior Computer Systems Validation (CSV Skillset) Location : Raritan, NJ (Onsite) Duration: 6 months Contract Job Description: Experience in computer systems validation, GXP regulatory knowledge and good documentation methods and CSA approaches and risk-based validation required. Prior experience in SAP ECC/S4 HANA system validation,...
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Senior Validation Specialist
2 weeks ago
Raritan, United States K-Tek Resourcing LLC Full timeJob Title : Senior Computer Systems Validation (CSV Skillset) Location : Raritan, NJ (Onsite) Duration: 6 months Contract In order to make an application, simply read through the following job description and make sure to attach relevant documents. Job Description: Experience in computer systems validation, GXP regulatory knowledge and good documentation...
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Contract Validation Analyst
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Senior Specialist
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Raritan, United States ClinChoice Full timeSenior Regulatory Affairs Specialist Consultant at ClinChoice (View all jobs) Raritan, New Jersey, United States Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds.... ClinChoice is searching for a...
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Senior Quality Engineer
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Raritan, United States GForce Life Sciences Full timeSenior Quality Engineer, Medical DevicesOur client has engaged GForce to identify a Senior Quality Engineer with in-depth understanding of medical device quality system requirements, with specific experience in applying the following: Medical Device product risk management, Medical devices process validation, and Medical Device Design...
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Senior Quality Engineer
7 days ago
Raritan, United States GForce Life Sciences Full timeSenior Quality Engineer, Medical DevicesOur client has engaged GForce to identify a Senior Quality Engineer with in-depth understanding of medical device quality system requirements, with specific experience in applying the following: Medical Device product risk management, Medical devices process validation, and Medical Device Design...
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Senior Manager, HMD OTC Capital
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Raritan, United States Capgemini Engineering Full timePosition Overview: We have 2 open roles. 1 for Junior Consultant (0-3 years), For Junior role we will also consider College Graduate who can be trained on the job. and 1 for Senior Consultant (3-8 Years)As a MES PAS-X MBR Modeler you will play a critical role in the design, implementation, and maintenance of our MBR using Werum PAS-X V2/V3. You will ensure...
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Sr. Regulatory Affairs Specialist
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Raritan, United States ClinChoice Full timeJob Title: Senior Regulatory Affairs Specialist Employment Type: Full Time or 1 year Contract with potential extension Location: Raritan, NJ (Selected candidate should be able to work 3 days every week at Raritan, NJ office). We are looking for Candidates with Proven experience in regulatory affairs in Class III medical devices and PMA submissions in this...
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Sr. Regulatory Affairs Specialist
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Director, Technical Accounting
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